TY - JOUR
T1 - Visceral adiposity is associated with altered myocardial glucose uptake measured by 18FDG-PET in 346 subjects with normal glucose tolerance, prediabetes, and type 2 diabetes
AU - Kim, Gyuri
AU - Jo, Kwanhyeong
AU - Kim, Kwang Joon
AU - Lee, Yong ho
AU - Han, Eugene
AU - Yoon, Hye jin
AU - Wang, Hye Jin
AU - Kang, Eun Seok
AU - Yun, Mijin
N1 - Publisher Copyright:
© 2015 Kim et al.
PY - 2015/11/4
Y1 - 2015/11/4
N2 - Background: The heart requires constant sources of energy mostly from free fatty acids (FFA) and glucose. The alteration in myocardial substrate metabolism occurs in the heart of diabetic patients, but its specific association with other metabolic variables remains unclear. We aimed to evaluate glucose uptake in hearts of subjects with normal glucose tolerance (NGT), prediabetes, and type 2 diabetes mellitus (T2DM) using [18F]-fluorodeoxyglucose-positron emission tomography (18FDG-PET) in association with visceral and subcutaneous adiposity, and metabolic laboratory parameters. Methods: A total of 346 individuals (NGT, n=76; prediabetes, n=208; T2DM, n=62) in a health promotion center of a tertiary hospital were enrolled. The fasting myocardial glucose uptake, and visceral and subcutaneous fat areas were evaluated using 18FDG-PET and abdominal computed tomography, respectively. Results: Myocardial glucose uptake was significantly decreased in subjects with T2DM compared to the NGT or prediabetes groups (p for trend=0.001). Multivariate linear regression analyses revealed that visceral fat area (β=-0.22, p=0.018), fasting FFA (β=-0.39, p<0.001), and uric acid levels (β=-0.21, p=0.007) were independent determinants of myocardial glucose uptake. Multiple logistic analyses demonstrated that decreased myocardial glucose uptake (OR 2.32; 95% CI 1.02-5.29, p=0.045) and visceral fat area (OR 1.02, 95% CI 1.01-1.03, p=0.018) were associated with T2DM. Conclusions: Our findings indicate visceral adiposity is strongly associated with the alteration of myocardial glucose uptake evaluated by 18FDG-PET, and its association further relates to T2DM.
AB - Background: The heart requires constant sources of energy mostly from free fatty acids (FFA) and glucose. The alteration in myocardial substrate metabolism occurs in the heart of diabetic patients, but its specific association with other metabolic variables remains unclear. We aimed to evaluate glucose uptake in hearts of subjects with normal glucose tolerance (NGT), prediabetes, and type 2 diabetes mellitus (T2DM) using [18F]-fluorodeoxyglucose-positron emission tomography (18FDG-PET) in association with visceral and subcutaneous adiposity, and metabolic laboratory parameters. Methods: A total of 346 individuals (NGT, n=76; prediabetes, n=208; T2DM, n=62) in a health promotion center of a tertiary hospital were enrolled. The fasting myocardial glucose uptake, and visceral and subcutaneous fat areas were evaluated using 18FDG-PET and abdominal computed tomography, respectively. Results: Myocardial glucose uptake was significantly decreased in subjects with T2DM compared to the NGT or prediabetes groups (p for trend=0.001). Multivariate linear regression analyses revealed that visceral fat area (β=-0.22, p=0.018), fasting FFA (β=-0.39, p<0.001), and uric acid levels (β=-0.21, p=0.007) were independent determinants of myocardial glucose uptake. Multiple logistic analyses demonstrated that decreased myocardial glucose uptake (OR 2.32; 95% CI 1.02-5.29, p=0.045) and visceral fat area (OR 1.02, 95% CI 1.01-1.03, p=0.018) were associated with T2DM. Conclusions: Our findings indicate visceral adiposity is strongly associated with the alteration of myocardial glucose uptake evaluated by 18FDG-PET, and its association further relates to T2DM.
KW - Insulin resistance
KW - Myocardium
KW - Positron emission tomography
KW - Type 2 diabetes mellitus
KW - Visceral fat
UR - https://www.scopus.com/pages/publications/84946200856
U2 - 10.1186/s12933-015-0310-4
DO - 10.1186/s12933-015-0310-4
M3 - Article
C2 - 26538247
AN - SCOPUS:84946200856
SN - 1475-2840
VL - 14
JO - Cardiovascular Diabetology
JF - Cardiovascular Diabetology
IS - 1
M1 - 148
ER -